Canonical Allele Identifier: CA993073618

Gene: C3

Linked Data

• gnomAD v3: 19-6710025-G-GAA
• gnomAD v4: 19-6710025-G-GAA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710025_6710026insAA , CM000681.2:g.6710025_6710026insAA	GRCh38
NC_000019.9:g.6710036_6710037insAA , CM000681.1:g.6710036_6710037insAA	GRCh37
NC_000019.8:g.6661036_6661037insAA	NCBI36
NG_009557.1:g.15626_15627insTT , LRG_27:g.15626_15627insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-184_1564-183insTT	ENSP00000512083.1:n.1564-184_1564-183insTT
ENST00000695654.1:c.811-184_811-183insTT	ENSP00000512085.1:n.811-184_811-183insTT
ENST00000695655.1:c.592-148_592-147insTT	ENSP00000512086.1:n.592-148_592-147insTT
ENST00000695692.1:n.1051-184_1051-183insTT
ENST00000245907.11:c.1687-184_1687-183insTT MANE Select	ENSP00000245907.4:n.1687-184_1687-183insTT
ENST00000245907.10:c.1687-184_1687-183insTT	ENSP00000245907.4:n.1687-184_1687-183insTT
ENST00000600763.1:n.320-184_320-183insTT
NM_000064.3:c.1687-184_1687-183insTT	NP_000055.2:n.1687-184_1687-183insTT
NM_000064.4:c.1687-184_1687-183insTT MANE Select	NP_000055.2:n.1687-184_1687-183insTT